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A systematic procedure to enhance reproducibility of SWASV cycles in the determination of toxic metals in real samples

机译:一种系统的程序,可提高SWASV循环在真实样品中有毒金属的测定中的重现性

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摘要

This work presents for the first time a systematic study on the optimization of the electrochemical cleaning time of a mercury film when it is used as a working electrode material in the analysis of toxic metals, such as Pb2+, used as model metal, in real samples by SWASV. The optimization study for the film’s cleaning time aimed at attaining a Pb2+ minimum value in the film after the re-oxidation step of the pre-concentrated metal, given the impossibility of complete removal of traces of the electroactive species from the film. This value was kept constant in each concentration range studied ensuring thus that all assays were performed in initial identical conditions. An assay performed on a synthetic sample was taken as reference. In it, given the absence of matrix effects, and after the electrochemical cleaning step, a direct proportionality was observed between the residual amounts of Pb2+ in the film (which for the cleaning time used was never completely removed) and Pb2+ concentration in the solution. This fact determined a high correlation between Pb2+ peak current and Pb2+ concentration which was not observed when real samples (tree leaves) were analyzed. This behavior may result from the presence of the interfering surfactants always present in real samples of complex matrix. Cleaning time optimization was performed for the following Pb2+ concentration ranges in the real samples of complex matrix: 0.006-0.020, 0.020-0.080, 0.060-0.200 and 0.100-0.600 ppb. As expected, in order to obtain identical levels of film’s cleaning efficiency, the need for longer cleaning times has been observed for higher concentrations. The optimized cleaning times for the concentration ranges under study were 120, 150, 180 e 300 s, respectively.
机译:这项工作首次对在实际样品中用作有毒金属(例如Pb2 +)的汞膜用作工作电极材料进行分析时,优化了汞膜的电化学清洗时间的优化的系统研究。由SWASV。针对膜清洁时间的优化研究旨在在预浓缩金属的再氧化步骤之后,使膜中的Pb2 +最小值达到最小值,因为不可能从膜中完全清除痕量的电活性物质。在所研究的每个浓度范围内,该值均保持恒定,从而确保所有测定均在初始相同条件下进行。对合成样品进行的测定作为参考。在其中,由于没有基体效应,并且在电化学清洗步骤之后,在膜中残留的Pb2 +量(对于所用的清洗时间从未完全去除)与溶液中的Pb2 +浓度之间存在直接的比例关系。这一事实确定了Pb2 +峰值电流与Pb2 +浓度之间的高度相关性,而在分析实际样品(树叶)时并未观察到这种相关性。此行为可能是由于复杂基质的实际样品中始终存在干扰性表面活性剂而导致的。在复杂基质的实际样品中,针对以下Pb2 +浓度范围执行了清洁时间优化:0.006-0.020、0.020-0.080、0.060-0.200和0.100-0.600 ppb。如所期望的,为了获得相同水平的薄膜清洁效率,对于更高的浓度,人们观察到需要更长的清洁时间。针对所研究浓度范围的最佳清洁时间分别为120、150、180和300 s。

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